HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479324Generated: October 26, 2026
Ammonium Chloride → 4,4-Di methyl-5alpha-cholesta-8,14,24-trien-3-one
https://huagongshe.com/reaction/479324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Isopropyltriphenylphosphonium bromide | HCID 2795292 | — |
| Reactant | 3-Oxo-4,4-dimethyl-5alpha-chola-8,14-dien-24-aldehyde | HCID 15543093 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178527699 | HCID 178527699 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-Di methyl-5alpha-cholesta-8,14,24-trien-3-one | HCID 70037746 | 51.7% |
| Product | HCID 178460676 | HCID 178460676 | — |
Reaction Steps
A solution of isopropyltriphenylphosphorane was prepared by addition of BuLi (0.16 ml of 1.6M in hexanes, 0.26 mmol) to a suspension of isopropyltriphenylphosphonium bromide (98 mg, 0.26 mmol) in THF (2 mL) at ice bath temperature. The corresponding deep red phosphorane solution was stirred a further 0.5 hour and then added dropwise via syringe to a solution of 3-oxo-4,4-dimethyl-5α-chola-8,14-dien-24-aldehyde (71 mg, 0.18 mmol) in THF (2ml) at −78° C. and stirred 2 hours before slowly warming to room temperature and stirring overnight. Saturated ammonium chloride (3 mL) was added and the aqueous phase extracted using diethyl ether, and the organic phase dried over anhydrous sodium sulphate. Flash chromatography (Eluant: 6 hexane: 1 ethyl acetate) gave the title compound (38 mg, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645953B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-06c62459272d4f0c8c49c09c42202482 |
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| Source note | uspto-grants-2003_11 |
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